The epidemiology of premature aging and associated comorbidities von Coppede, Fabio

Volltext

Searching for the role and the most suitable biomarkers of oxidative stress in Alzheimer's disease and in other neurodegenerative diseases von Migliore, L., Fontana, I., Colognato, R., Coppede, F., Siciliano, G., Murri, L.

Volltext

Environmental-induced oxidative stress in neurodegenerative disorders and aging von Migliore, Lucia, Coppedè, Fabio

Volltext

Folate gene polymorphisms and the risk of Down syndrome pregnancies in young Italian women von Coppedè, Fabio, Marini, Giulia, Bargagna, Stefania, Stuppia, Liborio, Minichilli, Fabrizio, Fontana, Ilaria, Colognato, Renato, Astrea, Guia, Palka, Giandomenico, Migliore, Lucia

Volltext

Oxidative DNA damage in peripheral leukocytes of mild cognitive impairment and AD patients von Migliore, L., Fontana, I., Trippi, F., Colognato, R., Coppedè, F., Tognoni, G., Nucciarone, B., Siciliano, G.

Volltext

Epigenetic effects of nano-sized materials von Stoccoro, Andrea, Karlsson, Hanna L, Coppedè, Fabio, Migliore, Lucia

Volltext

Association of micronucleus frequency with neurodegenerative diseases von Migliore, Lucia, Coppedè, Fabio, Fenech, Michael, Thomas, Philip

Volltext

DNA methylation of genes regulating appetite and prediction of weight loss after bariatric surgery in obese individuals von Coppedè, F., Seghieri, M., Stoccoro, A., Santini, E., Giannini, L., Rossi, C., Migliore, L., Solini, A.

Volltext

Genotoxicity induced by arsenic compounds in peripheral human lymphocytes analysed by cytokinesis-block micronucleus assay von Colognato, R, Coppedè, F, Ponti, J, Sabbioni, E, Migliore, L

Volltext

Increased expression of the Hutchinson-Gilford progeria syndrome truncated lamin A transcript during cell aging von Rodriguez, Sofia, Coppedè, Fabio, Sagelius, Hanna, Eriksson, Maria

Volltext

The complex relationship between folate/homocysteine metabolism and risk of Down syndrome von COPPEDE, Fabio

Volltext

Genetic and environmental factors in cancer and neurodegenerative diseases von Migliore, Lucia, Coppedè, Fabio

Volltext

Mutations Involved in Premature-Ageing Syndromes von Coppede, Fabio

Volltext

Folate, homocysteine, vitamin B12, and polymorphisms of genes participating in one-carbon metabolism in late-onset Alzheimer's disease patients and healthy controls von Coppedè, Fabio, Tannorella, Pierpaola, Pezzini, Ilaria, Migheli, Francesca, Ricci, Giulia, Caldarazzo lenco, Elena, Piaceri, Irene, Polini, Antonio, Nacmias, Benedetta, Monzani, Fabio, Sorbi, Sandro, Siciliano, Gabriele, Migliore, Lucia

Volltext

Susceptibility to chromosome malsegregation in lymphocytes of women who had a Down syndrome child in young age von Migliore, L., Boni, G., Bernardini, R., Trippi, F., Colognato, R., Fontana, I., Coppedè, F., Sbrana, I.

Volltext

Polymorphisms and haplotypes in folate-metabolizing genes and risk of non-Hodgkin lymphoma von Skibola, Christine F., Forrest, Matthew S., Coppedé, Fabio, Agana, Luz, Hubbard, Alan, Smith, Martyn T., Bracci, Paige M., Holly, Elizabeth A.

Volltext

A panel of in vitro tests to evaluate genotoxic and morphological neoplastic transformation potential on Balb/3T3 cells by pristine and remediated titania and zirconia nanoparticle... von Stoccoro, Andrea, Di Bucchianico, Sebastiano, Uboldi, Chiara, Coppedè, Fabio, Ponti, Jessica, Placidi, Claudia, Blosi, Magda, Ortelli, Simona, Costa, Anna Luisa, Migliore, Lucia

Volltext

Risk of Non–Hodgkin Lymphoma Associated with Polymorphisms in Folate-Metabolizing Genes von LIGHTFOOT, Tracy J, SKIBOLA, Christine F, WILLETT, Eleanor V, SKIBOLA, Danica R, ALLAN, James M, COPPEDE, Fabio, ADAMSON, Peter J, MORGAN, Gareth J, ROMAN, Eve, SMITH, Martyn T

Volltext

Modulation of hydrogen peroxide-induced DNA damage, MAPKs activation and cell death in PC12 by ergothioneine von Colognato, Renato, Laurenza, Incoronata, Fontana, Ilaria, Coppedé, Fabio, Siciliano, Gabriele, Coecke, Sandra, Aruoma, Okezie I., Benzi, Luca, Migliore, Lucia

Volltext

1922P Targeted resequencing designed specifically for thymic epithelial tumours confirmed the high prevalence of GTF2I mutations von Petrini, I., Pardini, E., Cucchiara, F., Sardo Infirri, G., Burzi, I.S., Barachini, S., Monatli, M., Maestri, M., Ricciardi, R., Nicolì, V., Coppedè, F., Bacchin, D., Melfi, F., Aprile, V., Lucchi, M.

Volltext